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The non-canonical Wnt receptor Ryk regulates hematopoietic stem cell repopulation in part by controlling proliferation and apoptosis

机译:非规范的Wnt受体Ryk部分通过控制增殖和凋亡来调节造血干细胞的再增殖

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The development of blood and immune cells requires strict control by various signaling pathways in order to regulate self-renewal, differentiation and apoptosis in stem and progenitor cells. Recent evidence indicates critical roles for the canonical and non-canonical Wnt pathways in hematopoiesis. The non-canonical Wnt pathway is important for establishment of cell polarity and cell migration and regulates apoptosis in the thymus. We here investigate the role of the non-canonical Wnt receptor Ryk in hematopoiesis and lymphoid development. We show that there are dynamic changes in Ryk expression during development and in different hematopoietic tissues. Functionally, Ryk regulates NK cell development in a temporal fashion. Moreover, Ryk-deficient mice show diminished, but not absent self-renewal of hematopoietic stem cells (HSC), via effects on mildly increased proliferation and apoptosis. Thus, Ryk deficiency in HSCs from fetal liver reduces their quiescence, leading to proliferation-induced apoptosis and decreased self-renewal.
机译:为了调节干细胞和祖细胞的自我更新,分化和凋亡,血液和免疫细胞的发育需要通过各种信号途径进行严格控制。最近的证据表明,经典和非经典Wnt通路在造血中起着关键作用。非经典的Wnt通路对于建立细胞极性和细胞迁移并调节胸腺的凋亡非常重要。我们在这里研究非典型Wnt受体Ryk在造血和淋巴发育中的作用。我们显示在发育过程中和在不同的造血组织中Ryk表达有动态变化。在功能上,Ryk以暂时的方式调节NK细胞的发育。此外,Ryk缺陷小鼠通过对轻度增加的增殖和凋亡的作用,显示出造血干细胞(HSC)的自我更新减弱,但不消失。因此,来自胎儿肝脏的HSC中的Ryk缺乏减少了它们的静止,导致了增殖诱导的细胞凋亡和自我更新的减少。

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